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Prognostic impact of diabetes mellitus on hepatocellular carcinoma: Special emphasis from the BCLC perspective

BACKGROUND: Diabetes mellitus (DM) is associated with higher incidence and poorer prognosis of hepatocellular carcinoma (HCC). The influence of DM on patient survival in different HCC stages is not known. METHODS: A prospective dataset of 3,182 HCC patients was collected between 2002 and 2014. Patie...

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Autores principales: Su, Yu-Wen, Liu, Po-Hong, Hsu, Chia-Yang, Lee, Yun-Hsuan, Hsia, Cheng-Yuan, Ho, Shu-Yein, Hou, Ming-Chih, Chen, Harn-Shen, Huo, Teh-Ia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363902/
https://www.ncbi.nlm.nih.gov/pubmed/28333991
http://dx.doi.org/10.1371/journal.pone.0174333
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author Su, Yu-Wen
Liu, Po-Hong
Hsu, Chia-Yang
Lee, Yun-Hsuan
Hsia, Cheng-Yuan
Ho, Shu-Yein
Hou, Ming-Chih
Chen, Harn-Shen
Huo, Teh-Ia
author_facet Su, Yu-Wen
Liu, Po-Hong
Hsu, Chia-Yang
Lee, Yun-Hsuan
Hsia, Cheng-Yuan
Ho, Shu-Yein
Hou, Ming-Chih
Chen, Harn-Shen
Huo, Teh-Ia
author_sort Su, Yu-Wen
collection PubMed
description BACKGROUND: Diabetes mellitus (DM) is associated with higher incidence and poorer prognosis of hepatocellular carcinoma (HCC). The influence of DM on patient survival in different HCC stages is not known. METHODS: A prospective dataset of 3,182 HCC patients was collected between 2002 and 2014. Patients were divided into three groups according to BCLC stages (BCLC stage 0 and stage A, BCLC stage B, BCLC stage C and stage D). We compared the cumulative survival rate of diabetic and non-diabetic patients in different BCLC groups. The correlation between DM and overall survival was also analyzed by multivariate Cox regression model within each group. RESULTS: DM is present in 25.2% of all patients. Diabetic patients had lower cumulative survival in BCLC stage 0 plus BCLC stage A group (log rank p<0.001), and BCLC stage B group (log rank p = 0.012), but not in BCLC stage C plus BCLC stage D group (log rank p = 0.132). Statistically significant differences in overall survival are found between diabetic and non-diabetic patients in BCLC stage 0 plus stage A group (adjusted hazard ratio [HR] = 1.45, 95% confidence interval [CI] 1.08–1.93, p = 0.013), and BCLC stage B (adjusted HR = 1.77, 95% CI 1.24–2.51, p = 0.002). In contrast, the survival difference is not seen in BCLC stage C plus stage D group (adjusted HR = 1.09, 95% CI 0.90–1.30, p = 0.387). CONCLUSIONS: DM is prevalent in HCC, and is associated with lower survival rate in HCC patients with BCLC stage 0 plus stage A and B, but not in those with BCLC stage C plus stage D.
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spelling pubmed-53639022017-04-06 Prognostic impact of diabetes mellitus on hepatocellular carcinoma: Special emphasis from the BCLC perspective Su, Yu-Wen Liu, Po-Hong Hsu, Chia-Yang Lee, Yun-Hsuan Hsia, Cheng-Yuan Ho, Shu-Yein Hou, Ming-Chih Chen, Harn-Shen Huo, Teh-Ia PLoS One Research Article BACKGROUND: Diabetes mellitus (DM) is associated with higher incidence and poorer prognosis of hepatocellular carcinoma (HCC). The influence of DM on patient survival in different HCC stages is not known. METHODS: A prospective dataset of 3,182 HCC patients was collected between 2002 and 2014. Patients were divided into three groups according to BCLC stages (BCLC stage 0 and stage A, BCLC stage B, BCLC stage C and stage D). We compared the cumulative survival rate of diabetic and non-diabetic patients in different BCLC groups. The correlation between DM and overall survival was also analyzed by multivariate Cox regression model within each group. RESULTS: DM is present in 25.2% of all patients. Diabetic patients had lower cumulative survival in BCLC stage 0 plus BCLC stage A group (log rank p<0.001), and BCLC stage B group (log rank p = 0.012), but not in BCLC stage C plus BCLC stage D group (log rank p = 0.132). Statistically significant differences in overall survival are found between diabetic and non-diabetic patients in BCLC stage 0 plus stage A group (adjusted hazard ratio [HR] = 1.45, 95% confidence interval [CI] 1.08–1.93, p = 0.013), and BCLC stage B (adjusted HR = 1.77, 95% CI 1.24–2.51, p = 0.002). In contrast, the survival difference is not seen in BCLC stage C plus stage D group (adjusted HR = 1.09, 95% CI 0.90–1.30, p = 0.387). CONCLUSIONS: DM is prevalent in HCC, and is associated with lower survival rate in HCC patients with BCLC stage 0 plus stage A and B, but not in those with BCLC stage C plus stage D. Public Library of Science 2017-03-23 /pmc/articles/PMC5363902/ /pubmed/28333991 http://dx.doi.org/10.1371/journal.pone.0174333 Text en © 2017 Su et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Su, Yu-Wen
Liu, Po-Hong
Hsu, Chia-Yang
Lee, Yun-Hsuan
Hsia, Cheng-Yuan
Ho, Shu-Yein
Hou, Ming-Chih
Chen, Harn-Shen
Huo, Teh-Ia
Prognostic impact of diabetes mellitus on hepatocellular carcinoma: Special emphasis from the BCLC perspective
title Prognostic impact of diabetes mellitus on hepatocellular carcinoma: Special emphasis from the BCLC perspective
title_full Prognostic impact of diabetes mellitus on hepatocellular carcinoma: Special emphasis from the BCLC perspective
title_fullStr Prognostic impact of diabetes mellitus on hepatocellular carcinoma: Special emphasis from the BCLC perspective
title_full_unstemmed Prognostic impact of diabetes mellitus on hepatocellular carcinoma: Special emphasis from the BCLC perspective
title_short Prognostic impact of diabetes mellitus on hepatocellular carcinoma: Special emphasis from the BCLC perspective
title_sort prognostic impact of diabetes mellitus on hepatocellular carcinoma: special emphasis from the bclc perspective
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363902/
https://www.ncbi.nlm.nih.gov/pubmed/28333991
http://dx.doi.org/10.1371/journal.pone.0174333
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